Pilot Study : New Sensors to Monitor Apnea During Sedation (JAWAC)
Primary Purpose
Sleep Apnea, Obstructive, Anesthesia
Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
JAWAC system + Capnoline + Spo2
Sponsored by
About this trial
This is an interventional diagnostic trial for Sleep Apnea, Obstructive focused on measuring Propofol, Deep Sedation, Anoxia, Hypercapnia
Eligibility Criteria
Inclusion Criteria:
- Any adult patient scheduled for a sleep apnea provocation test under sedation by propofol
- Hospital Erasme during the period of the study.
Exclusion Criteria:
- Patient Refusal
- Patient Age: 18 years and under 80 years
- Intervention earlier in the mandible or thorax
- A history of facial burn
- Allergy tape
Sites / Locations
- Erasme Hospital
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
ALL INCLUDED PATIENTS
Arm Description
A single arm for this study. All the patients benefit of both systems. The participants are their own control. Non invasive sensors are used to monitor and record data of those two systems in a synchron way ( JAWAC / Capnoline + Spo2).
Outcomes
Primary Outcome Measures
Optimal JAWAC signal threshold detecting obstructive apnea
The apnea is defined clinically by the anesthesiologist with the help of the capnoLine/Spo2. The purpose is to define the optimal signal detection during a continuous record of the system JAWAC associated with the occurrence of obstructive apnea.
The results will give a variation in centimeters for a certain amount of time. It is possible that the optimal signal detection will be a combination of different sensors.
The sensibility, specificity versus precocity of the signal will be studied.
Secondary Outcome Measures
Time limit between the detection of each system and the episode of désaturation
The assumption is that the signal JAWAC enable an earlier response of the anesthetist and a priori reduce the occurrence of desaturation at the onset of obstructive apnea compared to the capnoLine/spo2 system.
Full Information
NCT ID
NCT02909309
First Posted
September 13, 2016
Last Updated
August 22, 2018
Sponsor
Erasme University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02909309
Brief Title
Pilot Study : New Sensors to Monitor Apnea During Sedation
Acronym
JAWAC
Official Title
Pilot Study : Evaluation of a Mandibular and Abdominal Motion Detection Sensors (JAWAC) to Prevent Apnea During Sedation With Propofol in TCI Mode
Study Type
Interventional
2. Study Status
Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
March 1, 2017 (Actual)
Primary Completion Date
July 31, 2017 (Actual)
Study Completion Date
July 31, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Erasme University Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Evaluation of a Mandibular and Abdominal Motion Detection Sensor (JAWAC) to Prevent Apnea During Sedation With Propofol in TCI Mode
Detailed Description
In 2016 , monitoring of propofol sedation , currently recommended by the American Society of Anaesthesiology and European companies includes among others, a pulse oximeter (SpO2) and a continuous measurement of CO2 exhaled by an appropriate device (CapnoLine). This monitoring does not allow to anticipate the occurrence of obstructive apnea .
The anticipation of the occurrence of apnea or airway obstruction using this type of monitoring could allow the anesthesiologist to act earlier on the titration of propofol and maintaining the airway. This would avoid the side effects associated with hypoxemia and hypercapnia and therefore further improve patient safety .
This pilot study tests the JAWAC system to detect those apneas.
This is an interventional diagnostic study on the JAWAC monitoring system validation in a prospective cohort of patients undergoing sedation in order to provoke sleep apnea. Indeed , sedation technique is already used with propofol during snoring provocation tests in patients at risk for sleep apnea.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Apnea, Obstructive, Anesthesia
Keywords
Propofol, Deep Sedation, Anoxia, Hypercapnia
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
21 (Actual)
8. Arms, Groups, and Interventions
Arm Title
ALL INCLUDED PATIENTS
Arm Type
Other
Arm Description
A single arm for this study. All the patients benefit of both systems. The participants are their own control.
Non invasive sensors are used to monitor and record data of those two systems in a synchron way ( JAWAC / Capnoline + Spo2).
Intervention Type
Device
Intervention Name(s)
JAWAC system + Capnoline + Spo2
Intervention Description
measure mandibular mouvements + etCO2 + pulse oxymetry, respectively
Primary Outcome Measure Information:
Title
Optimal JAWAC signal threshold detecting obstructive apnea
Description
The apnea is defined clinically by the anesthesiologist with the help of the capnoLine/Spo2. The purpose is to define the optimal signal detection during a continuous record of the system JAWAC associated with the occurrence of obstructive apnea.
The results will give a variation in centimeters for a certain amount of time. It is possible that the optimal signal detection will be a combination of different sensors.
The sensibility, specificity versus precocity of the signal will be studied.
Time Frame
at time of anesthesia
Secondary Outcome Measure Information:
Title
Time limit between the detection of each system and the episode of désaturation
Description
The assumption is that the signal JAWAC enable an earlier response of the anesthetist and a priori reduce the occurrence of desaturation at the onset of obstructive apnea compared to the capnoLine/spo2 system.
Time Frame
at time of anesthesia
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Any adult patient scheduled for a sleep apnea provocation test under sedation by propofol
Hospital Erasme during the period of the study.
Exclusion Criteria:
Patient Refusal
Patient Age: 18 years and under 80 years
Intervention earlier in the mandible or thorax
A history of facial burn
Allergy tape
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luc Barvais
Organizational Affiliation
Erasme University Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Erasme Hospital
City
Brussels
ZIP/Postal Code
1070
Country
Belgium
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
2508510
Citation
Tinker JH, Dull DL, Caplan RA, Ward RJ, Cheney FW. Role of monitoring devices in prevention of anesthetic mishaps: a closed claims analysis. Anesthesiology. 1989 Oct;71(4):541-6. doi: 10.1097/00000542-198910000-00010.
Results Reference
background
PubMed Identifier
18232350
Citation
Senny F, Destine J, Poirrier R. Midsagittal jaw movement analysis for the scoring of sleep apneas and hypopneas. IEEE Trans Biomed Eng. 2008 Jan;55(1):87-95. doi: 10.1109/TBME.2007.899351.
Results Reference
background
PubMed Identifier
25232693
Citation
Niklewski PJ, Phero JC, Martin JF, Lisco SJ. A novel index of hypoxemia for assessment of risk during procedural sedation. Anesth Analg. 2014 Oct;119(4):848-856. doi: 10.1213/ANE.0000000000000371.
Results Reference
background
PubMed Identifier
30610518
Citation
Ponthieu N, Coeckelenbergh S, Engelman E, Tuna T, Van Obbergh L, Barvais L. Synchronized mandibular movement and capnography: a novel approach to obstructive airway detection during procedural sedation-a post hoc analysis of a prospective study. J Clin Monit Comput. 2019 Dec;33(6):1065-1070. doi: 10.1007/s10877-018-00250-3. Epub 2019 Jan 4.
Results Reference
derived
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Pilot Study : New Sensors to Monitor Apnea During Sedation
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